RS267608465 MECP2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
Inborn genetic diseases
Syndromic X-linked intellectual disability Lubs type
X-linked intellectual disability-psychosis-macroorchidism syndrome
Autism
susceptibility to
X-linked 3
MECP2-related disorder
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
Inborn genetic diseases
Syndromic X-linked intellectual disability Lubs type
X-linked intellectual disability-psychosis-macroorchidism syndrome
Autism
Other Variants in MECP2